Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Polymer electrolytes with high Li-ion conductivity provide a route toward improved safety and performance of Li-ion batteries. However, most polymer electrolytes suffer from low ionic conduction and an even lower Li-ion contribution to the conductivity (the transport number, ), with the anion typically transporting over 80% of the charge. Here, we show that subtle and potentially undetected associations within a polymer electrolyte can entrain both the anion and the cation. When removed, the conductivity performance of the electrolyte can be improved by almost 2 orders of magnitude. Importantly, while some of this improvement can be attributed to a decreased glass transition temperature, , the removal of the amide functional group reduces interactions between the polymer and the Li cations, doubling the Li to 0.43, as measured using pulsed-field-gradient NMR. This work highlights the importance of strategic synthetic design and emphasizes the dual role of and ion binding for the development of polymer electrolytes with increased total ionic conductivity and the Li ion contribution to it.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acsmacrolett.0c00788 | DOI Listing |
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